Canonical Allele Identifier: CA2067685711
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997513A= , CM000674.2:g.120997513A= GRCh38
NC_000012.11:g.121435316A= , CM000674.1:g.121435316A= GRCh37
NC_000012.10:g.119919699A= NCBI36
NG_011731.2:g.23768A= , LRG_522:g.23768A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*96A= ENSP00000453965.2:n.*96A=
ENST00000257555.11:c.1349A= MANE Select ENSP00000257555.5:p.Asn450=
ENST00000257555.10:c.1349A= ENSP00000257555.4:p.Asn450=
ENST00000400024.6:c.1349A= ENSP00000476181.1:p.Asn450=
ENST00000402929.5:n.2215A=
ENST00000535955.5:n.65A=
ENST00000538626.2:n.213A=
ENST00000538646.5:c.*325A= ENSP00000443964.1:n.*325A=
ENST00000540108.1:c.*789A= ENSP00000445445.1:n.*789A=
ENST00000541395.5:c.1349A= ENSP00000443112.1:p.Asn450=
ENST00000541924.5:c.*363A= ENSP00000440361.1:n.*363A=
ENST00000543255.1:n.393A=
ENST00000543427.5:c.812A= ENSP00000439721.2:p.Asn271=
ENST00000544413.2:c.1349A= ENSP00000438804.1:p.Asn450=
ENST00000544574.5:c.*112A= ENSP00000438565.1:n.*112A=
ENST00000560968.5:c.1166A=
ENST00000615446.4:c.137A= ENSP00000483994.1:p.Asn46=
ENST00000617366.4:c.587-121A= ENSP00000481967.1:n.587-121A=
NM_000545.5:c.1349A= , LRG_522t1:c.1349A= NP_000536.5:p.Asn450=
NM_000545.6:c.1349A= NP_000536.5:p.Asn450=
NM_001306179.1:c.1349A= NP_001293108.1:p.Asn450=
XM_005253931.2:c.1349A= XP_005253988.1:p.Asn450=
XM_024449168.1:c.1349A= XP_024304936.1:p.Asn450=
NM_000545.8:c.1349A= MANE Select NP_000536.6:p.Asn450=
NM_001306179.2:c.1349A= NP_001293108.2:p.Asn450=